HDE supplement
H160002 S007: PulseRider Aneurysm Neck Reconstruction Device
FDA HDE supplement · 30-day notice · Medos International, SARL
Key facts
| Original HDE | H160002 |
|---|---|
| Supplement number | S007 |
| Supplement type | 30-day notice |
| Reason for the supplement | process change - manufacturer/sterilizer/packager/supplier |
| Trade name | PulseRider Aneurysm Neck Reconstruction Device |
| Generic name | Intracranial neurovascular stent |
| Applicant | Medos International, SARL |
| Product code | NJE |
| Received date | Feb 22, 2019 |
| Decision date | Mar 21, 2019 |
At a glance
- No Approval order on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About HDE supplements
An HDE supplement asks FDA to approve a change to a Humanitarian Use Device that already holds a humanitarian device exemption.
Source: U.S. Food and Drug Administration (FDA), Humanitarian Device Exemption (HDE) database · Source date: